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Enzymatic asymmetric synthesis of chiral amino acids

Journal

CHEMICAL SOCIETY REVIEWS
Volume 47, Issue 4, Pages 1516-1561

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7cs00253j

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Funding

  1. National Natural Science Foundation of China [31170761, 21476210]

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Chiral amino acids are extensively applied in the pharmaceutical, food, cosmetic, agricultural, and feedstuff industries. The development of synthetic methodologies for optically pure amino acids has been driven by their significant applications. Among the various synthesis methods for the production of chiral amino acids, enzymatic asymmetric synthesis is a unique preparation strategy that shows great potential. This review provides an overview of the reported methods for enzymatic asymmetric synthesis of chiral amino acids, including asymmetric reductive amination of keto acids, asymmetric transfer of an amino group to keto acids, enantioselective addition of ammonia to alpha,beta-unsaturated acids, and aldol condensation of an amino acid to aldehydes.

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